Associate Director LBA
Mattawan, MI · On-site
Utilizing these platforms/assays, the teams are responsible for the method development, validation ... Effectively plan, assign and direct work within one operational area with expanded scope and/or ...
Mattawan, MI · On-site
Utilizing these platforms/assays, the teams are responsible for the method development, validation ... Effectively plan, assign and direct work within one operational area with expanded scope and/or ...
Mattawan, MI · On-site
Utilizing these platforms/assays, the teams are responsible for the method development, validation ... Effectively plan, assign and direct work within one operational area with expanded scope and/or ...
Utilizing these platforms/assays, the teams are responsible for the method development, validation ... Effectively plan, assign and direct work within one operational area with expanded scope and/or ...
Utilizing these platforms/assays, the teams are responsible for the method development, validation ... Effectively plan, assign and direct work within one operational area with expanded scope and/or ...
As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy ... Drive analytical validation plans (e.g., accuracy, precision, sensitivity/specificity, LoD ...
As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy ... Drive analytical validation plans (e.g., accuracy, precision, sensitivity/specificity, LoD ...
The Global Development IT (GD IT) Associate Director, Product Lead is a leader within the GD ... Intake, assess, prioritize, and validate domain requirements in partnership with BSPs, managing ...
The Global Development IT (GD IT) Associate Director, Product Lead is a leader within the GD ... Intake, assess, prioritize, and validate domain requirements in partnership with BSPs, managing ...
Travere Therapeutics in San Diego (remote-friendly, hybrid) seeks an Associate Director, Quality Assurance - Technical. Lead GxP analytical QA, oversee method qualification/validation, and interact ...
New
Travere Therapeutics in San Diego (remote-friendly, hybrid) seeks an Associate Director, Quality Assurance - Technical. Lead GxP analytical QA, oversee method qualification/validation, and interact ...
New
Interlochen, MI · On-site +1
$60K/yr
The Associate Director of Admission Operations (AD) plays a critical role in ensuring that the ... Manage high-stakes decision release processes, including data validation, testing, and final ...
Quick apply
Interlochen, MI · On-site +1
$60K/yr
The Associate Director of Admission Operations (AD) plays a critical role in ensuring that the ... Manage high-stakes decision release processes, including data validation, testing, and final ...
Role Summary The Associate Director, Program Portfolio Lead - Research Programs is responsible for ... validation, portfolio prioritization, and transition into platform development. This role is ...
Role Summary The Associate Director, Program Portfolio Lead - Research Programs is responsible for ... validation, portfolio prioritization, and transition into platform development. This role is ...
This position reports to the Associate Director, Data Integrity. Essential Functions (Essential ... execute validation and perform other project-related work. 10% Execute protocols for routine ...
This position reports to the Associate Director, Data Integrity. Essential Functions (Essential ... execute validation and perform other project-related work. 10% Execute protocols for routine ...
POSITION SUMMARY Associate Directors play an essential role in preparing for Board of Directors ... A valid state issued ID and reliable transportation are also necessary for this position. Salary ...
POSITION SUMMARY Associate Directors play an essential role in preparing for Board of Directors ... A valid state issued ID and reliable transportation are also necessary for this position. Salary ...
When a Director position becomes available, the Board's Nominating Committee prioritizes filling ... A valid state issued ID and reliable transportation are also necessary for this position.
When a Director position becomes available, the Board's Nominating Committee prioritizes filling ... A valid state issued ID and reliable transportation are also necessary for this position.
POSITION SUMMARY Associate Directors play an essential role in preparing for Board of Directors ... A valid state issued ID and reliable transportation are also necessary for this position.
Quick apply
POSITION SUMMARY Associate Directors play an essential role in preparing for Board of Directors ... A valid state issued ID and reliable transportation are also necessary for this position.
Associate Director Pharmacometrics Programming provides timely support to the study team on all ... The evaluation and development of study requirements and validation plan are also in the scope of ...
Associate Director Pharmacometrics Programming provides timely support to the study team on all ... The evaluation and development of study requirements and validation plan are also in the scope of ...
Detroit, MI · On-site +1
$77K - $154K/yr
Description The Associate Director - Corporate Specialty and Govt Banking Portfolio Manager will ... Recruiting agencies must have a valid, written and fully executed Master Service Agreement and ...
Detroit, MI · On-site +1
$77K - $154K/yr
Description The Associate Director - Corporate Specialty and Govt Banking Portfolio Manager will ... Recruiting agencies must have a valid, written and fully executed Master Service Agreement and ...
Detroit, MI · On-site +1
$77K - $154K/yr
Description The Associate Director - Corporate Specialty and Govt Banking Portfolio Manager will ... Recruiting agencies must have a valid, written and fully executed Master Service Agreement and ...
Detroit, MI · On-site +1
$77K - $154K/yr
Description The Associate Director - Corporate Specialty and Govt Banking Portfolio Manager will ... Recruiting agencies must have a valid, written and fully executed Master Service Agreement and ...
... enter/validate data in our donor database and other tracking sheets. In addition, the assistant ... Support the associate director of individual stewardship with annual endowment reporting and ...
... enter/validate data in our donor database and other tracking sheets. In addition, the assistant ... Support the associate director of individual stewardship with annual endowment reporting and ...
Detroit, MI · On-site
$50K/yr
This position reports to the Associate Director, Data Integrity. Essential Functions (Essential ... execute validation and perform other project-related work. 10% Execute protocols for routine ...
Detroit, MI · On-site
$50K/yr
This position reports to the Associate Director, Data Integrity. Essential Functions (Essential ... execute validation and perform other project-related work. 10% Execute protocols for routine ...
Thought Leader Marketing Liaison (TLML) (Associate Director) is a key member of the Immunology ... Valid driver's license.Candidates must live in or near geographical area and should reside near a ...
Thought Leader Marketing Liaison (TLML) (Associate Director) is a key member of the Immunology ... Valid driver's license.Candidates must live in or near geographical area and should reside near a ...
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
Big Rapids, MI · On-site
$24.79/hr
Position reports to the Associate Vice President for Advancement/Executive Director of The Ferris ... Valid Driver's License Physical Demands: * Office Environment * Moving * Reaching * Sitting
| Aspect | Associate Director Validation | Validation Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Engineering, or related fields; often requires industry certifications | Bachelor's or Master's in similar fields; certifications like ASQ or ISPE are common |
| Work Environment | Leads validation teams, oversees validation strategies, and collaborates with cross-functional departments | Manages validation projects, ensures compliance, and reports to senior management |
| Employer & Industry Usage | Pharmaceutical, biotech, and medical device industries; used in large organizations | Similar industries; common in mid to large-sized companies for validation oversight |
The Associate Director Validation typically holds a higher strategic role, overseeing validation teams and strategies, while the Validation Manager focuses on managing validation projects and ensuring compliance. Both roles require similar credentials and are vital in regulated industries, but the Associate Director has broader leadership responsibilities.
Other
Medical, Retirement, PTO
This job post has expired today. Applications are no longer accepted.
8.4
Based on 94 frontline employees who took The Breakroom Quiz
22nd of 86 rated pharmaceutical
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies.
Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:
Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:
Physical Demands:
The pay range for this position is $135-150k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location
Work Environment:
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Scientific research and development services
10,000+ Employees
Wilmington, MA, US
1947